NDC 48951-8318

Purple Coneflower

Purple Coneflower

Purple Coneflower is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Sage; Calendula Officinalis Flowering Top; Echinacea Pallida; Eucalyptus Globulus Leaf; Mercuric Cyanide; Silver Nitrate; Atropa Belladonna; Silicon Dioxide.

Product ID48951-8318_55134586-07b9-2b76-e054-00144ff8d46c
NDC48951-8318
Product TypeHuman Otc Drug
Proprietary NamePurple Coneflower
Generic NamePurple Coneflower
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc
Substance NameSAGE; CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA PALLIDA; EUCALYPTUS GLOBULUS LEAF; MERCURIC CYANIDE; SILVER NITRATE; ATROPA BELLADONNA; SILICON DIOXIDE
Active Ingredient Strength1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-8318-2

360 SPRAY in 1 BOTTLE, SPRAY (48951-8318-2)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-8318-2 [48951831802]

Purple Coneflower SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
SAGE1 [hp_X]/1

OpenFDA Data

SPL SET ID:86dc3350-36b6-11df-9879-0800200c9a66
Manufacturer
UNII

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